The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
115040448 11504044 8 F 2011 20160909 20150914 20160914 EXP PHHY2015BR104865 NOVARTIS 75.06 YR F Y 49.00000 KG 20160914 MD BR BR

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
115040448 11504044 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 1 DF, QMO 21008 1 DF SUSPENSION /month
115040448 11504044 2 C METFORMIN METFORMIN HYDROCHLORIDE 1 Oral 2 DF, QD 0 2 DF TABLET QD
115040448 11504044 3 C ATENOLOL. ATENOLOL 1 Oral 2 DF, QD 0 2 DF TABLET QD
115040448 11504044 4 C HYDRALAZINE HYDRALAZINE HYDROCHLORIDE 1 Oral 1 DF, QD 0 1 DF TABLET QD
115040448 11504044 5 C AMLODIPINE AMLODIPINE BESYLATE 1 Oral 2 DF, QD 0 2 DF TABLET QD
115040448 11504044 6 C OMEPRAZOLE. OMEPRAZOLE 1 Oral 1 DF, QD 0 1 DF TABLET QD
115040448 11504044 7 C ASA ASPIRIN 1 Oral 100 MG, QD 0 100 MG QD
115040448 11504044 8 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 Oral 1 DF, QD 0 1 DF TABLET QD
115040448 11504044 9 C NIFEDIPINE. NIFEDIPINE 1 Oral 2 DF, QD 0 2 DF TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115040448 11504044 1 Neuroendocrine tumour
115040448 11504044 2 Diabetes mellitus
115040448 11504044 3 Hypertension
115040448 11504044 4 Hypertension
115040448 11504044 5 Hypertension
115040448 11504044 6 Gastritis erosive
115040448 11504044 7 Cardiac disorder
115040448 11504044 8 Hypertension
115040448 11504044 9 Hypertension

Outcome of event

Event ID CASEID OUTC COD
115040448 11504044 HO
115040448 11504044 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
115040448 11504044 Abdominal adhesions
115040448 11504044 Abdominal discomfort
115040448 11504044 Abdominal distension
115040448 11504044 Abdominal pain
115040448 11504044 Blood cholesterol increased
115040448 11504044 Blood creatinine increased
115040448 11504044 Burning sensation
115040448 11504044 Concomitant disease aggravated
115040448 11504044 Confusional state
115040448 11504044 Diarrhoea
115040448 11504044 Disorientation
115040448 11504044 Disturbance in attention
115040448 11504044 Drug ineffective
115040448 11504044 Dysgeusia
115040448 11504044 Erythema
115040448 11504044 Hepatic function abnormal
115040448 11504044 Hypersensitivity
115040448 11504044 Hypoaesthesia
115040448 11504044 Joint swelling
115040448 11504044 Laziness
115040448 11504044 Malaise
115040448 11504044 Malignant neoplasm progression
115040448 11504044 Nausea
115040448 11504044 Neoplasm progression
115040448 11504044 Pain
115040448 11504044 Peripheral swelling
115040448 11504044 Pruritus
115040448 11504044 Rash
115040448 11504044 Rash papular
115040448 11504044 Recurrent cancer
115040448 11504044 Scratch
115040448 11504044 Sleep disorder
115040448 11504044 Swelling
115040448 11504044 Tumour pain
115040448 11504044 Vomiting
115040448 11504044 Wound

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
115040448 11504044 1 2010 0
115040448 11504044 2 2010 0
115040448 11504044 7 2010 0